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Targeting nanoparticles across the blood-brain barrier with monoclonal antibodies
被引:0
|作者:
Loureiro, Joana A.
[1
]
Gomes, Barbara
[1
]
Coelho, Manuel A. N.
[1
]
Pereira, Maria do Carmo
[1
]
Rocha, Sandra
[2
]
机构:
[1] Univ Porto, Dept Chem Engn, LEBABE, Fac Engn, P-4200465 Oporto, Portugal
[2] Chalmers Univ Technol, Dept Chem & Biol Engn, SE-41296 Gothenburg, Sweden
来源:
关键词:
Alzheimer's disease;
blood-brain barrier;
liposome;
monoclonal antibody;
Parkinson's disease;
PLGA nanoparticles;
targeting;
ANTITRANSFERRIN RECEPTOR ANTIBODY;
STERICALLY STABILIZED LIPOSOMES;
ENABLE DRUG-DELIVERY;
AMYLOID-BETA PEPTIDE;
TRANSFERRIN-RECEPTOR;
IN-VIVO;
ALZHEIMERS-DISEASE;
GENE-THERAPY;
ELECTRICAL-RESISTANCE;
PARKINSONS-DISEASE;
D O I:
10.2217/NNM.14.27
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Development of therapeutics for brain disorders is one of the more difficult challenges to be overcome by the scientific community due to the inability of most molecules to cross the blood-brain barrier (BBB). Antibody-conjugated nanoparticles are drug carriers that can be used to target encapsulated drugs to the brain endothelial cells and have proven to be very promising. They significantly improve the accumulation of the drug in pathological sites and decrease the undesirable side effect of drugs in healthy tissues. We review the systems that have demonstrated promising results in crossing the BBB through receptor-mediated endocytic mechanisms for the treatment of neurodegenerative disorders such as Alzheimer's and Parkinson's disease.
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页码:709 / 722
页数:14
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